sulphuric(IV) acid 512
s
CuO(s) + H 2 SO 4 (l) →CuSO 4 (aq) +
H 2 O(l)
It is also a powerful dehydrating
agent, capable of removing H 2 O from
many organic compounds (as in the
production of acid *anhydrides). In
dilute solution it is a strong dibasic
acid forming two series of salts, the
sulphates and the hydrogensul-
phates.
sulphuric(IV) acidSee sulphurous
acid.
sulphur monochlorideSee disul-
phur dichloride.
sulphur mustard A chemical war-
fare agent, C 4 H 8 Cl 2 S; r.d. 1.27; m.p.
14.4°C; b.p. 217°C. It is a potent blis-
tering agent,Ürst used in 1915 by
Germany in World War I. It is often
known simply as mustard gas, al-
though it is an oily liquid, which can
be dispersed as an aerosol. It was one
of the early chemicals used in chemo-
therapy treatment of cancer. The sys-
tematic name is bis(2-chlorethyl)
sulphide. See also nitrogen mustard.
sulphurous acid (sulphuric(IV) acid)
A weak dibasic acid, H 2 SO 3 , known in
the form of its salts: the sulphites
and hydrogensulphites. It is consid-
ered to be formed (along with sul-
phuric acid) when sulphur dioxide is
dissolved in water. It is probable,
however, that the molecule H 2 SO 3 is
not present and that the solution
contains hydrated SO 2. It is a reduc-
ing agent. The systematic name is
trioxosulphuric(IV) acid. See also sul-
phuric acid.
sulphur(IV) oxideSee sulphur
dioxide.
sulphur(VI) oxideSee sulphur
trioxide.
sulphur trioxide (sulphur(VI)
oxide)A colourless fuming solid,
SO 3 , which has three crystalline
modiÜcations. In decreasing order of
stability these are: α, r.d. 1.97; m.p.
16.83°C; b.p. 44.8°C; β, m.p. 16.24°C;
sublimes at 50°C; r.d. 2.29; γ, m.p.
16.8°C; b.p. 44.8°C. All are polymeric,
with linked SO 4 tetrahedra: the γ-
form has an icelike structure and is
obtained by rapid quenching of the
vapour; the β-form has inÜnite heli-
cal chains; and the α-form has in-
Ünite chains with some cross-linking
of the SO 4 tetrahedra. Even in the
vapour, there are polymeric species,
and not discrete sulphur trioxide
molecules (hence the compound is
more correctly called by its system-
atic name sulphur(VI) oxide).
Sulphur trioxide is prepared by the
oxidation of sulphur dioxide with
oxygen in the presence of a vana-
dium(V) oxide catalyst. It may be pre-
pared in the laboratory by distilling a
mixture of concentrated sulphuric
acid and phosphorus(V) oxide. It re-
acts violently with water to give sul-
phuric(VI) acid and is an important
intermediate in the preparation of
sulphuric acid and oleum.
sulphuryl chlorideSee sulphur
dichloride dioxide.
sulphuryl group The group =SO 2 ,
as in *sulphur dichloride oxide.
O
O
S
Cl
Cl
sulphuryl
group
sulphur (VI) dichloride
dioxide O
Cl
Cl
sulphur (IV) dichloride
oxide
S
thionyl
group
Sulphuryl group